A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055114



Internal ID19144333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22300068hg38UCSC Ensembl
Innerchr15:20564575..22588019hg19UCSC Ensembl
Innerchr15:18824589..20089383hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381940747
hg192023445
hg181264795
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2191n100
Supporting Variantsnssv3537607, nssv3713789, nssv3537612, nssv3537605, nssv3713790, nssv3537613, nssv3537608, nssv3537610, nssv3713788, nssv3537614, nssv3537606, nssv3537609, nssv3537616, nssv3713792, nssv3537611, nssv3537615, nssv3537604, nssv3713791
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055114
Frequency
Sample Size11257
Observed Gain15
Observed Loss3
Observed Complex0
Frequencyn/a


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